Canonical Allele Identifier: CA475204397

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703868T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936400T>C , CM000673.2:g.68936400T>C	GRCh38
NC_000011.9:g.68703868T>C , CM000673.1:g.68703868T>C	GRCh37
NC_000011.8:g.68460444T>C	NCBI36
NG_007976.1:g.37550T>C , LRG_250:g.37550T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1920T>C MANE Select	ENSP00000255078.4:p.Phe640=
ENST00000674675.1:c.164T>C
ENST00000674878.1:c.164T>C
ENST00000674955.1:c.*637T>C	ENSP00000502463.1:n.*637T>C
ENST00000675118.1:c.1408T>C
ENST00000675389.1:n.195T>C
ENST00000675615.1:c.1920T>C	ENSP00000502413.1:p.Phe640=
ENST00000675648.1:n.1295T>C
ENST00000675916.1:c.164T>C
ENST00000676173.1:n.2665T>C
ENST00000676182.1:c.351T>C
ENST00000676228.1:c.*1243T>C	ENSP00000502375.1:n.*1243T>C
ENST00000255078.7:c.1920T>C	ENSP00000255078.3:p.Phe640=
ENST00000539064.5:n.1679T>C
ENST00000543739.5:n.913T>C
ENST00000545475.1:n.516T>C
NM_002180.2:c.1920T>C , LRG_250t1:c.1920T>C	NP_002171.2:p.Phe640=
XM_005273974.2:c.909T>C	XP_005274031.1:p.Phe303=
XM_005273975.2:c.792T>C	XP_005274032.1:p.Phe264=
XM_011544994.1:c.687T>C	XP_011543296.1:p.Phe229=
XR_949903.1:n.2022T>C
XM_005273975.3:c.792T>C	XP_005274032.1:p.Phe264=
XM_017017669.2:c.909T>C	XP_016873158.1:p.Phe303=
XM_017017670.2:c.909T>C	XP_016873159.1:p.Phe303=
XR_949903.3:n.2018T>C
NM_002180.3:c.1920T>C MANE Select	NP_002171.2:p.Phe640=